Suppr超能文献

莱施-奈恩病:从机制到模型再回归

Lesch-Nyhan disease: from mechanism to model and back again.

作者信息

Jinnah H A

机构信息

Departments of Neurology and Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Dis Model Mech. 2009 Mar-Apr;2(3-4):116-21. doi: 10.1242/dmm.002543.

Abstract

Lesch-Nyhan disease (LND) is a rare inherited disorder caused by mutations in the gene encoding hypoxanthine-guanine phosphoribosyltransferase (HPRT). LND is characterized by overproduction of uric acid, leading to gouty arthritis and nephrolithiasis. Affected patients also have characteristic neurological and behavioral anomalies. Multiple cell models have been developed to study the molecular and metabolic aspects of LND, and several animal models have been developed to elucidate the basis for the neurobehavioral syndrome. The models have different strengths and weaknesses rendering them suitable for studying different aspects of the disease. The extensive modeling efforts in LND have questioned the concept that an 'ideal' disease model is one that replicates all of its features because the pathogenesis of different elements of the disease involves different mechanisms. Instead, the modeling efforts have suggested a more fruitful approach that involves developing specific models, each tailored for addressing specific experimental questions.

摘要

莱施-奈恩综合征(LND)是一种罕见的遗传性疾病,由编码次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HPRT)的基因突变引起。LND的特征是尿酸过度产生,导致痛风性关节炎和肾结石。受影响的患者还具有特征性的神经和行为异常。已经开发了多种细胞模型来研究LND的分子和代谢方面,并且已经开发了几种动物模型来阐明神经行为综合征的基础。这些模型有不同的优缺点,使其适合于研究该疾病的不同方面。LND广泛的建模工作对“理想”疾病模型是复制其所有特征这一概念提出了质疑,因为该疾病不同要素的发病机制涉及不同的机制。相反,建模工作提出了一种更有成效的方法,即开发特定的模型,每个模型都针对解决特定的实验问题进行定制。

相似文献

1
Lesch-Nyhan disease: from mechanism to model and back again.
Dis Model Mech. 2009 Mar-Apr;2(3-4):116-21. doi: 10.1242/dmm.002543.
2
Transcriptomic approach to Lesch-Nyhan disease.
Nucleosides Nucleotides Nucleic Acids. 2014;33(4-6):208-17. doi: 10.1080/15257770.2014.880477.
4
Management of neurological symptoms in Lesch-Nyhan disease: A systematic review.
Neurosci Biobehav Rev. 2024 Oct;165:105847. doi: 10.1016/j.neubiorev.2024.105847. Epub 2024 Aug 6.
5
Genotypic and phenotypic spectrum in attenuated variants of Lesch-Nyhan disease.
Mol Genet Metab. 2014 Aug;112(4):280-5. doi: 10.1016/j.ymgme.2014.05.012. Epub 2014 May 28.
6
Molecular, biochemical, and genetic characterization of a female patient with Lesch-Nyhan disease.
Mol Genet Metab. 2006 Mar;87(3):249-52. doi: 10.1016/j.ymgme.2005.09.025. Epub 2005 Dec 15.

引用本文的文献

1
Psychiatric Manifestations in Children and Adolescents with Inherited Metabolic Diseases.
J Clin Med. 2024 Apr 10;13(8):2190. doi: 10.3390/jcm13082190.
3
EpiTyping: analysis of epigenetic aberrations in parental imprinting and X-chromosome inactivation using RNA-seq.
Nat Protoc. 2023 Dec;18(12):3881-3917. doi: 10.1038/s41596-023-00898-5. Epub 2023 Nov 1.
5
Stem Cell-Based Therapeutic Approaches in Genetic Diseases.
Adv Exp Med Biol. 2023;1436:19-53. doi: 10.1007/5584_2023_761.
6
Case report: Early-onset renal failure as presenting sign of Lesch-Nyhan disease in infancy.
Front Pediatr. 2022 Dec 19;10:1080486. doi: 10.3389/fped.2022.1080486. eCollection 2022.
7
Lesch-Nyhan disease causes impaired energy metabolism and reduced developmental potential in midbrain dopaminergic cells.
Stem Cell Reports. 2021 Jul 13;16(7):1749-1762. doi: 10.1016/j.stemcr.2021.06.003. Epub 2021 Jul 1.
8
Human de novo purine biosynthesis.
Crit Rev Biochem Mol Biol. 2021 Feb;56(1):1-16. doi: 10.1080/10409238.2020.1832438. Epub 2020 Nov 12.
9
Animal Model Contributions to Congenital Metabolic Disease.
Adv Exp Med Biol. 2020;1236:225-244. doi: 10.1007/978-981-15-2389-2_9.

本文引用的文献

1
Animal models for drug discovery in dystonia.
Expert Opin Drug Discov. 2008 Jan;3(1):83-97. doi: 10.1517/17460441.3.1.83.
2
3
Consequences of impaired purine recycling in dopaminergic neurons.
Neuroscience. 2008 Mar 27;152(3):761-72. doi: 10.1016/j.neuroscience.2007.10.065. Epub 2008 Jan 17.
5
A human neuronal tissue culture model for Lesch-Nyhan disease.
J Neurochem. 2007 May;101(3):841-53. doi: 10.1111/j.1471-4159.2007.04472.x.
6
Basal ganglia dopamine loss due to defect in purine recycling.
Neurobiol Dis. 2007 May;26(2):396-407. doi: 10.1016/j.nbd.2007.01.010. Epub 2007 Feb 8.
7
Nifedipine suppresses self-injurious behaviors in animals.
Dev Neurosci. 2007;29(3):241-50. doi: 10.1159/000096414. Epub 2006 Oct 17.
8
Delineation of the motor disorder of Lesch-Nyhan disease.
Brain. 2006 May;129(Pt 5):1201-17. doi: 10.1093/brain/awl056. Epub 2006 Mar 20.
9
Behavioral aspects of Lesch-Nyhan disease and its variants.
Dev Med Child Neurol. 2005 Oct;47(10):673-7. doi: 10.1017/S0012162205001374.
10
A Golgi study of neuronal architecture in a genetic mouse model for Lesch-Nyhan disease.
Neurobiol Dis. 2005 Nov;20(2):479-90. doi: 10.1016/j.nbd.2005.04.005.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验